SEC61G在浸润性乳腺癌中的表达及意义

王艳; 刘先富; 许波; 张波

doi:10.16766/j.cnki.issn.1674-4152.002566

SEC61G在浸润性乳腺癌中的表达及意义

doi: 10.16766/j.cnki.issn.1674-4152.002566

蚌埠医学院第一附属医院肿瘤外科，安徽蚌埠 233004

基金项目:

安徽省教育厅重点课题 KJ2019A0341

蚌埠医学院自然科学重点项目 BYKY2019127ZD

详细信息

通讯作者:
张波, E-mail: 2684508656@qq.com

中图分类号: R737.9
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- 被引次数: 0
出版历程
- 收稿日期: 2021-11-10
- 网络出版日期: 2022-09-23

Expression and significance of SEC61G in invasive breast cancer

Department of Oncology, the First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui 233004, China

摘要

摘要: 目的利用癌症基因组图谱(TCGA)数据库中的数据分析SEC61G在浸润性乳腺癌中的表达情况及其与临床预后的关系。方法从TCGA数据库中收集1 222个浸润性乳腺癌患者的RNAseq数据，用Wilcoxon秩和检验分析SEC61G在正常组织和肿瘤组织中表达的差异，采用logistic回归分析SEC61G的表达与临床病理特征的关系，使用Kaplan-Meier方法和Cox回归分析评估SEC61G在预后中的作用。结果浸润性乳腺癌组织中SEC61G的表达明显高于正常乳腺组织(P < 0.001)。T分期(P=0.028)、N分期(P=0.009)、病理分期(P=0.003)、ER状态(P < 0.001)、PR状态(P < 0.001)、HER2状态(P=0.025)、组织学类型(P < 0.001)与SEC61G表达显著相关。单因素Cox回归分析显示SEC61G高表达与DSS有相关性(P < 0.001，HR=0.426，95% CI=0.272~0.668)。多因素Cox分析显示SEC61G高表达是疾病特异生存率(DSS)的独立危险因素(P=0.009，HR=0.479，95% CI=0.276~0.831)。SEC61G的表达与浸润性乳腺癌的免疫浸润程度有关(P < 0.05)。各组的K-M曲线显示肿瘤组织中SEC61G表达越高浸润性乳腺癌患者的预后越差(P < 0.05)。结论 SEC61G高表达与浸润性乳腺癌预后不良有关，可以作为预测浸润性乳腺癌患者生存有效的生物标志物。
- SEC61γ亚基 /
- 浸润性乳腺癌 /
- 预后
Abstract: Objective To analyze the expression of SEC61G in invasive breast cancer from tumor Genome Map (TCGA) database and its relationship with clinical prognosis. Methods The RNAseq data of 1 222 patients with invasive breast cancer were collected from TCGA database. Wilcoxon rank sum test was used to analyze the difference of SEC61G expression between normal and tumor tissues. Logistic regression was used to analyze the relationship between SEC61G expression and clinicopathological features. Kaplan-Meier method and Cox regression analysis were used to evaluate the role of SEC61G in prognosis. Results The expression of SEC61G in invasive breast cancer was significantly higher than that in normal breast tissue (P < 0.001). T stage (P=0.028), N stage (P=0.009), pathological stage (P=0.003), ER status (P < 0.001), PR status (P < 0.001), HER2 status (P=0.025) and histological type (P < 0.001) were significantly correlated with SEC61G expression. Univariate Cox regression analysis showed that the high expression of SEC61G was associated with DSS (P < 0.001, HR=0.426, 95% CI: 0.272-0.668). Multivariate Cox analysis showed that high expression of SEC61G was an independent risk factor for DSS (P=0.009, HR=0.479, 95% CI: 0.276-0.831). The K-M curve of each group showed that the higher the expression of SEC61G in tumor tissue, the worse the prognosis of invasive breast cancer patients (P < 0.05). Conclusion The high expression of SEC61G is related to the poor prognosis of invasive breast cancer and can be used as an effective biomarker to predict the survival of patients with invasive breast cancer.
- SEC61G /
- Invasive breast cancer /
- Prognosis

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图 1 SEC61G在浸润性乳腺癌组织及正常组织中的表达情况

注：A为SEC61G在浸润性乳腺癌患者肿瘤组织和非配对正常组织中的表达；B为SEC61G在浸润性乳腺癌患者配对组织中的表达；C为SEC61G的ROC曲线显示其对肿瘤与正常组织有良好的区别能力。

Figure 1. SEC61G expression in invasive breast cancer and normal tissues

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图 2 SEC61G高表达组和低表达组OS、DSS、PFI的K-M曲线及各亚组的K-M曲线

注：SEC61G高表达组和低表达组的OS、DSS、PFI的K-M曲线依次为A~C; T分期、N分期、M分期、病理分期各亚组SEC61G高表达组和低表达组的OS的K-M曲线依次为D~G。

Figure 2. K-M curve of OS, DSS, PFI and K-M curve of each subgroup in SEC61G high expression group and low expression group

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图 3 SEC61G基因表达与免疫浸润相关性分析

Figure 3. Analysis of the relationship between SEC61G gene expression and immune infiltration

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表 1 TCGA数据库中SEC61G高表达组和低表达组的基线特征[例(%)]

Table 1. Baseline characteristics of SEC61G high expression group and low expression group in TCGA database [cases (%)]

临床特征	分类	SEC61G高表达	SEC61G低表达	χ²值	P值
总数		541	542
T分期	T1	154(28.6)	123(22.7)	11.862	0.008
	T2	297(55.1)	332(61.4)
	T3	77(14.3)	62(11.5)
	T4	11(2.0)	24(4.4)
N分期	N0	266(50.3)	248(46.4)	8.491	0.037
	N1	184(34.8)	174(32.5)
	N2	52(9.8)	64(12.0)
	N3	27(5.1)	49(9.2)
M分期	M0	462(98.7)	440(96.9)	2.729	0.099
	M1	6(1.3)	14(3.1)
病理分期	Ⅰ期	108(20.6)	73(13.6)	14.313	0.003
	Ⅱ期	301(57.4)	318(59.3)
	Ⅲ期	111(21.2)	131(24.4)
	Ⅳ期	4(0.8)	14(2.6)
组织学类型	浸润性导管癌	353(72.3)	419(85.7)	25.452	< 0.001
	浸润性小叶癌	135(27.7)	70(14.3)
PR状态	阴性	132(25.2)	210(41.1)		< 0.001^a
	未确定	1(0.2)	3(0.6)
	阳性	390(74.6)	298(58.3)
ER状态	阴性	79(15.1)	161(31.4)		< 0.001^a
	未确定	2(0.4)	0
	阳性	442(84.5)	351(68.6)
HER2状态	阴性	295(80.4)	263(73.1)	5.471	0.065
	未确定	5(1.4)	7(1.9)
	阳性	67(18.3)	90(25.0)
注：TCGA数据库中不是所有的RNAseq都有临床信息，存在1个患者测多次的情况。TCGA数据库中不是所有的临床变量的信息都完全，或多或少存在有缺失。^a为采用Fisher精确检验。

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表 2 SEC61G的表达与临床病理特征的关系

Table 2. Relationship between expression of SEC61G and clinicopathological features

临床特征	数目	OR(95% CI)	P值
T分期(T2~4 vs. T1)	1 080	1.359(1.034~1.791)	0.028
N分期(N0~1 vs. N2~3)	1 064	0.656(0.477~0.898)	0.009
M分期(M1 vs. M0)	922	2.450(0.974~6.970)	0.069
病理分期(Ⅰ vs. Ⅱ~Ⅳ)	1 060	0.607(0.437~0.839)	0.003
年龄(>60岁vs. ≤60岁)	1 083	0.967(0.761~1.229)	0.786
PR状态(阳性vs.阴性)	1 030	0.480(0.368~0.625)	< 0.001
ER状态(阳性vs.阴性)	1 033	0.390(0.287~0.526)	< 0.001
HER2状态(阳性vs.阴性)	715	1.507(1.056~2.159)	0.025
原发肿瘤部位(右vs.左)	1 083	0.859(0.677~1.091)	0.213
组织学类型(浸润性小叶癌vs.浸润性导管癌)	977	0.437(0.315~0.601)	< 0.001

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表 3 DSS的单因素Cox回归分析

Table 3. Univariate Cox regression analysis of DSS

临床特征	数目	HR(95% CI)	P值
T分期(T2~4 vs.T1)	1 059	0.562(0.326~0.968)	0.038
N分期(N0~1 vs.N2~3)	1 044	2.462(1.502~4.036)	< 0.001
病理分期(Ⅰ vs.Ⅱ~Ⅳ)	1 041	3.396(1.478~7.803)	0.004
PR状态(阳性vs.阴性)	1 010	1.926(1.238~2.997)	0.004
ER状态(阳性vs.阴性)	1 013	1.788(1.122~2.850)	0.015
组织类型(小叶癌vs.导管癌)	958	2.125(1.018~4.434)	0.045
SEC61G(高表达vs.低表达)	1 062	0.426(0.272~0.668)	< 0.001

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表 4 DSS的多因素Cox回归分析

Table 4. Multivariate Cox regression analysis of DSS

临床特征	数目	HR(95%CI)	P值
T分期(T2~4 vs.T1)	1 059	1.048(0.444~2.474)	0.914
N分期(N0~1 vs.N2~3)	1 044	3.337(1.911~5.826)	< 0.001
病理分期(Ⅰ vs. Ⅱ~Ⅳ)	1 041	1.847(0.574~5.939)	0.303
PR状态(阳性vs.阴性)	1 010	1.598(0.784~3.257)	0.197
ER状态(阳性vs.阴性)	1 013	1.151(0.537~2.466)	0.717
组织类型(小叶癌vs.导管癌)	958	2.067(0.858~4.976)	0.105
SEC61G(高表达vs.低表达)	1 062	0.479(0.276~0.831)	0.009

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